{{Rsnum
|rsid=121909244
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PPARG
|position=12434111
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPARG
}}{{omim
|id=601487
|rsnum=121909244
|variant=0007
}}{{ClinVar
|rsid=121909244
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=12475610
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PPARG:5468
|GENE_NAME=PPARG
|GENE_ID=5468
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.12475610C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601487.0007
|CLNSIG=5
|CLNCUI=C1720861
|CLNDBN=Lipodystrophy, familial partial, type 3
|Disease=Lipodystrophy
|CLNACC=RCV000008612.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1720861:604367:79083
}}